You are not alone

Being a family member, loved one or caregiver of someone with epilepsy and seizures can be challenging.  You want so badly to be able to help, to stop the seizure, to know "the right thing to do".

The pressure of caring for someone with epilepsy can seem overwhelming at times. From ensuring medications are taken everyday and on time, to administering first aid during a seizure, to attending doctor's appointments... the tasks of a caregiver can seem endless. It is important that caregivers do not neglect to take proper care of themselves. After all, you must be at your best to be able to care for another person.
Talking with other caregivers may help relieve the stress you might feel as a caregiver. Connect with other caregivers and loved ones of people with epilepsy on our eCommunities site where we have a Friends, Family, & Loved Ones forum.

At the Epilepsy Foundation of Minnesota, we provide programs and services to help you learn about epilepsy, to help you connect with others going through the same thing, to help you get involved, get active and take action.

If you are looking for specific caregiver support groups click here to search by county.

This website is for you.  Cruise through the pages, and if you don't see what you need, please call us at 651.287.2310 | 1.800.779.0777 ext. 2310.

About epilepsy

How to respond to a seizure

Programs that will help you connect with others

Epilogues Writing Collection

Stroll for Epilepsy

Volunteer Opportunities